Jit
Enthusiast computational biologist with business dream !!!
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Assistant Professor at GAUHATI UNIVERSITY, GUWAHATI
Advt. No.T/2014/4 Ref. No. GU/Estt/T/308(VI)/2014/6451-61 Applications are invited from the Indian citizens for five (5) teaching posts of Assistant Professor (Contractual) under various departments of Gauhati University. Details of the...Choosing the Right NGS Sequencing Instrument for Your Study
By Neel 1363 days agogenohub.com - The right sequencing instrument for your study depends on your project goal. Setting aside turnaround time and price, it essentially comes down to the numbers of reads and read length you need for your experiment. Below, we've described and compared...China University of Macau PhD Position 2015 in Bioinformatics, Computer Science
The Computational Biology and Bioinformatics Group at the University of Macau is inviting applications for PhD Position. Applicants will work on a research project focusing on the flexible receptor protein-ligand docking algorithms for...Common steps for reads mapping !
By BioStar 1096 days agoMapping reads to a reference genome is an essential step in many types of genomic analysis, such as variant calling and gene expression analysis.JNU Neuroscience/Systems Biology/Mathematical modeling JRF Vacancies
School of Computational and Integrative Sciences Jawaharlal Nehru University New Delhi 110067 Recruitment for Project Applications were invited from the citizens of India for filling up the following temporary position for the CSIR sponsored...1mb long DNA with Nanopore technology
By Jit 3001 days agoLongest read of 1mb achievements with NanoporeNanoPack: visualizing and processing long-read sequencing data
By Jit 2630 days agogithub.com - The NanoPack tools are written in Python3 and released under the GNU GPL3.0 License. The source code can be found at https://github.com/wdecoster/nanopack, together with links to separate scripts and their documentation. The scripts are compatible...Illumina Smartphone Chip !!!
By Robert M Willioms 4086 days agoIllumina, the company that claims it brought human genome sequencing down to $1000 prices, has now turned its attention to a consumer product - a chip that you can plug into your smartphone and have it read your genetic information.Kevler: Reference-free variant discovery in large eukaryotic genomes
By Jit 2232 days agogithub.com - Welcome to kevlar, software for predicting de novo genetic variants without mapping reads to a reference genome! kevlar's k-mer abundance based method calls single nucleotide variants (SNVs), multinucleotide variants (MNVs),...WALK-IN-INTERVIEW for the post of JRF and Project Assistant @ CIFT
Eligible candidates are invited to attend a walk-in-Interview with all relevant documents for the following positions of Project Fellows (on contractual basis) to work in the Project “ Genetic Diversity of Clostridium botulinum in seafood and...
